U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Nucleotide

Items: 1 to 20 of 7686

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6131224insertion1nstd186human GRCh37 chr15: 29,261,354-29,261,363 , GRCh38.p12 chr15|NT_187660.1: 1,244,101-1,244,110 , GRCh38.p12 chr15: 28,969,151-28,969,160 , GRCh38.p12 chr15|NW_011332701.1: 1,131,617-1,131,626 APBA2
    nsv6131181insertion1nstd186human GRCh37 chr15: 28,248,697-28,248,697 , GRCh38.p12 chr15: 28,003,551-28,003,551 , GRCh38.p12 chr15|NW_011332701.1: 137,847-137,847 , GRCh38.p12 chr15|NT_187660.1: 137,847-137,847 OCA2
    nsv6130428insertion1nstd186human GRCh37 chr15: 30,465,469-30,465,529 , GRCh38.p12 chr15: 30,173,266-30,173,326 , GRCh38.p12 chr15|NT_187660.1: 2,458,214-2,458,274 , GRCh38.p12 chr15|NW_011332701.1: 2,345,730-2,345,790 LOC105370746
    nsv6130335insertion1nstd186human GRCh37 chr15: 30,465,464-30,465,551 , GRCh38.p12 chr15|NW_011332701.1: 2,345,725-2,345,812 , GRCh38.p12 chr15: 30,173,261-30,173,348 , GRCh38.p12 chr15|NT_187660.1: 2,458,209-2,458,296 LOC105370746
    nsv6130311insertion1nstd186human GRCh37 chr15: 31,338,471-31,338,481 , GRCh38.p12 chr15|NT_187660.1: 3,332,027-3,332,037 , GRCh38.p12 chr15: 31,046,268-31,046,278 , GRCh38.p12 chr15|NW_011332701.1: 3,219,575-3,219,585 TRPM1
    nsv6129605insertion1nstd186human GRCh37 chr15: 29,423,793-29,423,803 , GRCh38.p12 chr15|NW_011332701.1: 1,293,735-1,293,745 , GRCh38.p12 chr15|NT_187660.1: 1,406,219-1,406,229 , GRCh38.p12 chr15: 29,131,590-29,131,600 ENTREP2
    nsv6123197copy number variation1nstd186human GRCh37 chr15: 30,774,640-30,787,077 , GRCh38.p12 chr15: 30,482,437-30,494,874 , GRCh38.p12 chr15|NW_011332701.1: 2,643,876-2,656,313 WHAMMP4
    nsv6122759copy number variation1nstd186human GRCh37 chr15: 32,536,733-32,537,036 , GRCh38.p12 chr15: 32,244,532-32,244,835 , GRCh38.p12 chr15|NT_187660.1: 4,530,221-4,530,522 , GRCh38.p12 chr15|NW_011332701.1: 4,417,769-4,418,070 , LOC102724078
    nsv6122751copy number variation1nstd186human GRCh37 chr15: 28,937,926-28,939,315 , GRCh38.p12 chr15: 28,692,780-28,694,169 , GRCh38.p12 chr15|NT_187660.1: 968,570-969,957 , GRCh38.p12 chr15|NW_011332701.1: 854,784-856,171 0
    nsv6122014copy number variation1nstd186human GRCh37 chr15: 31,839,278-31,839,330 , GRCh38.p12 chr15: 31,547,075-31,547,127 , GRCh38.p12 chr15|NT_187660.1: 3,832,227-3,832,279 , GRCh38.p12 chr15|NW_011332701.1: 3,719,775-3,719,827 OTUD7A
    nsv6121360copy number variation1nstd186human GRCh37 chr15: 29,648,310-29,648,508 , GRCh38.p12 chr15: 29,356,106-29,356,304 , GRCh38.p12 chr15|NW_011332701.1: 1,519,106-1,519,305 , GRCh38.p12 chr15|NT_187660.1: 1,631,590-1,631,789 ENTREP2
    nsv6117527mobile element insertion1nstd186human GRCh37 chr15: 29,820,920-29,820,971 , GRCh38.p12 chr15: 29,528,716-29,528,767 , GRCh38.p12 chr15|NT_187660.1: 1,804,213-1,804,264 , GRCh38.p12 chr15|NW_011332701.1: 1,691,729-1,691,780 ENTREP2
    nsv6117200mobile element insertion1nstd186human GRCh37 chr15: 28,179,364-28,179,364 , GRCh38.p12 chr15|NW_011332701.1: 68,505-68,505 , GRCh38.p12 chr15|NT_187660.1: 68,505-68,505 , GRCh38.p12 chr15: 27,934,218-27,934,218 OCA2
    nsv6116770copy number variation1nstd186human GRCh37 chr15: 31,137,777-31,139,021 , GRCh38.p12 chr15: 30,845,574-30,846,818 , GRCh38.p12 chr15|NT_187660.1: 3,131,303-3,132,547 , GRCh38.p12 chr15|NW_011332701.1: 3,018,851-3,020,095 0
    nsv6116397mobile element insertion1nstd186human GRCh37 chr15: 31,067,048-31,067,099 , GRCh38.p12 chr15|NW_011332701.1: 2,948,122-2,948,173 , GRCh38.p12 chr15|NT_187660.1: 3,060,574-3,060,625 , GRCh38.p12 chr15: 30,774,845-30,774,896 0
    nsv6115591mobile element insertion1nstd186human GRCh37 chr15: 31,157,754-31,157,805 , GRCh38.p12 chr15|NW_011332701.1: 3,038,815-3,038,866 , GRCh38.p12 chr15|NT_187660.1: 3,151,267-3,151,318 , GRCh38.p12 chr15: 30,865,551-30,865,602 0
    nsv6115248mobile element insertion1nstd186human GRCh37 chr15: 28,997,439-28,997,490 , GRCh38.p12 chr15: 28,752,293-28,752,344 , GRCh38.p12 chr15|NT_187660.1: 1,028,082-1,028,133 , GRCh38.p12 chr15|NW_011332701.1: 914,296-914,347 WHAMMP2
    nsv6115070mobile element insertion1nstd186human GRCh37 chr15: 29,023,034-29,023,085 , GRCh38.p12 chr15: 28,777,888-28,777,939 , GRCh38.p12 chr15|NT_187660.1: 1,053,680-1,053,731 , GRCh38.p12 chr15|NW_011332701.1: 939,894-939,945 0
    nsv5672819copy number variation1nstd102humanPathogenic GRCh37 chr15: 31,355,301-31,369,124 , GRCh38.p12 chr15|NT_187660.1: 3,348,868-3,362,668 , GRCh38.p12 chr15: 31,063,098-31,076,921 , GRCh38.p12 chr15|NW_011332701.1: 3,236,416-3,250,216 TRPM1, MIR211
    nsv5672736copy number variation1nstd102humanPathogenic GRCh37 chr15: 28,263,523-28,263,723 , GRCh38.p12 chr15: 28,018,377-28,018,577 , GRCh38.p12 chr15|NT_187660.1: 152,677-152,877 , GRCh38.p12 chr15|NW_011332701.1: 152,677-152,877 OCA2
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center